Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 67520303 | HCID 67520303 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86062305 | HCID 86062305 | — |
Reaction Steps
A mixture of 6-(2-carbamoylpyridin-4-yloxy)-1-napthoic acid (Step a, 1.0 g, 3.2 mmol) and SOCl2 (600 μL, 8.1 mmol) in toluene (25 mL, Aldrich) was heated at 110° C. for 7 h. The solution was concentrated under reduced pressure and azeotroped from toluene (3×10 mL) to provide the title compounds as a yellow solid. MS (ESI, pos. ion) m/z: 327.5 (M+1). Mass Calc'd for C17H11ClN2O3: 326.73.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07435823B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-b2f50db6c86a44a2a993413bf1e2f28d |
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| Source note | uspto-grants-2008_10 |
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